Results 101 to 110 of about 6,450 (193)
Summary of published mutations in MSX1 gene.
, 2018 Summary of published mutations in MSX1 gene.
Vladimir J. Balcar (5728256) +9 more
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Genetics and Molecular Biology, 2006 Cleft lip and/or palate (CL/P) is a major congenital defect with complex etiology, including multiple genetic and environmental factors. Approximately two thirds of the cases are not accompanied by other anomalies and are called nonsyndromic (NS). In the
Aline Lourenço da Silva +4 more
doaj +1 more source
Msx1 Mutations And Their Binding Interactions
, 2013 Orofacial clefting (OFC), also called cleft lip and/or palate, is the most common congenital birth anomaly that involve the craniofacial region in humans.
Prakash, Divakar
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Defective Msx1 Nuclear Translocation Underlies Severe Oligodontia
International Dental JournalAim or purpose: This study aimed to elucidate the mechanism by which MSX1 variants contribute to nonsyndromic tooth agenesis (NSTA) and determine how variant domains correlate with tooth loss severity.
Jing Sun, Chen Yiqi, Zhang Caiqi
doaj +1 more source
A human MSX1 homeodomain missense mutation causes selective tooth agenesis
, 1996 We demonstrate that a mutation in the homeobox gene, MSX1, causes a common developmental anomaly, familial tooth agenesis. Genetic linkage analyses in a family with autosomal dominant agenesis of second premolars and third molars identified a locus on ...
Karimbux N. +4 more
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Msx1 genomic binding associates with enrichment of the H3K9me2 repressive mark in myoblast cells.
, 2012 (A) Diagram of six Msx1 repressed target genes [23] showing the positions of Msx1 binding sites and known regulatory regions as well as their overlap; also shown is a negative control site. DRR: Distal Regulatory Region.
Jingqiang Wang (6502) +1 more
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Msx1 and Pax3 Cooperate to Mediate FGF8 and WNT Signals during Xenopus Neural Crest Induction
, 2005 SummaryFGF, WNT, and BMP signaling promote neural crest formation at the neural plate boundary in vertebrate embryos. To understand how these signals are integrated, we have analyzed the role of the transcription factors Msx1 and Pax3.
Estee Wang +5 more
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Dental agenesis: review of the literature and report of two cases
Revista Facultad de Odontología Universidad de Antioquia, 2006 Tooth agenesis is the most common anomaly of craniofacial development. The purpose of this report is to present a brief review of literature about tooth agenesis, which includes: terminology, etiology, prevalence, associated syndromes and dental ...
Luz Ángela Arboleda-A. +8 more
doaj
MSX1, PAX9, and TGFA contribute to tooth agenesis in humans.
, 2004 In this study, we sought to determine the association between tooth agenesis and DNA sequence variation in the genes MSX1 and PAX9 in an ethnically diverse human population.
Meira, R +3 more
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Characterization of the gene product of the MSX1 gene with the c.452-9G>A substitution.
, 2015 (A) Immunolocalization of FLAG-tagged MSX1 protein in transfected COS7 cells. Nuclear translocation (wild-type) is disrupted by c.452-9G>A substitution in the intronic region (mutant).
Kazuo Shimozato (610781) +12 more
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